Associate Manager/Manager CDM(Study Manager) - Remote U.S/Canada
Company: Thermo Fisher Scientific
Location: Greenville
Posted on: August 7, 2022
Job Description:
We are vital links between an idea for a new medicine and the
people who need it. We are the people of PPD - thousands of
employees in locations worldwide connected by tenacity and passion
for our purpose: to improve health. You will be joining a truly
collaborative and winning culture as we strive to bend the time and
cost curve of delivering life-saving therapies to patients. - -Are
you a data and a people person? Here's your team. We manage and
clean the data collected in a clinical trial - from the design and
build of the database and edit checks, through the entry and
cleaning of data to the final delivery of clinical trial data. We
work closely with the project teams and clients to identify best
practices and processes, meet and exceed our clients' needs, and do
the right thing to earn their trust. -As an Associate
-Manager/Manager of Clinical Data Management(Early Phase), you will
help ensure the success of your team and CDM Projects. You will
work to provide training, mentorship and guideance. This includes
but not limited to interviewing new staff, performance management,
reviewing and approving time and expense reports. This role is also
considered a study manager in which you will be responsible for
managing active CDM Projects from start to finish in Early
Development. -At PPD we hire the best, develop ourselves and each
other, and recognize the power of being one team. We offer
continued career advancement opportunities, award winning training
and benefits focused on the health and wellbeing of our
employees.Summarized Purpose:Manages project staff and workload of
direct reports. Responsible for training, mentoring, and guiding
project staff and direct reports within a portfolio.Essential
Functions:
- Manages staff, which may include interviewing and selection,
job description preparation, professional development, goal
setting, performance management, coaching and mentoring, employee
counseling, and separations. Approves courses of action on salary
administration, hiring, corrective action, and terminations.
Reviews and approves time records, expense reports, requests for
leave, and overtime. -
- Provides support, oversight and coaching to the DM team to
ensure that all tasks are completed accurately, on time and within
budget to meet or exceed client expectations. -
- Ensures staff compliance with documented procedures. May
monitor, evaluate and propose mitigation strategies surrounding
risk to deliverables. -
- Assists with implementation of operational activities of study
or portfolios, with focus on quality in order to better support
study manager. -
- Participates in the development and implementation of
processes, procedures and training for the data management
function. -
- Manages resourcing (allocations) for all assigned staff within
DM portfolio, includes global resourcing reporting and strategizing
with senior management.Education/Experience:
- Bachelor's degree or equivalent and relevant formal academic /
vocational qualification
- Previous experience that provides the knowledge, skills, and
abilities to perform the job (comparable to 0 to -5+ years).
Expereince should be within a Clinical, Pharma, or CRO
-environment. Successful candidates should be familar with EDC
systems and/or CDM activities.
- 1+ year of leadership responsibility
- In some cases an equivalency, consisting of a combination of
appropriate education, training and/or directly related experience,
will be considered sufficient for an individual to meet the
requirements of the role. -Knowledge, Skills & Abilities:
- Ability to effectively apply knowledge and skills in a highly
organized fashion while adhering to regulatory guidelines, SOPs and
client expectations
- Strong attention to detail and skill with numbers
- Strong written and verbal communication skills with strong
command of English language and grammar
- Strong analytical/problem-solving skills
- Ability to maintain a high degree of confidentiality with
clinical data and client's proprietary data -
- Strong customer focus and excellent interpersonal skills -
- Ability to act as a study or department expert for DM
processes
- Ability to effectively manage and motivate others and to
effectively supervise and delegate tasks -
- Ability to set and meet, for self and team, timelines or be
able to recognize and schedule changes in response to project
demandsWorking Environment:PPD values the health and wellbeing of
our employees. We support and encourage individuals to create a
healthy and balanced environment where they can thrive. - Below is
listed the working environment/requirements for this role: -
- Able to communicate, receive, and understand information and
ideas with diverse groups of people in a comprehensible and
reasonable manner. -
- Able to work upright and stationary for typical working hours.
- -
- Ability to use and learn standard office equipment and
technology with proficiency. -
- Able to perform successfully under pressure while prioritizing
and handling multiple projects or activities. - -
- May require travel. 10-20% annual possible. -
- Employees hired in this role may be assigned to a US government
contract and if so would be subject to COVID-19 vaccination and
reporting requirements.PPD Defining Principles:We have a strong
will to win - We earn our customer's trust - We are gamechangers -
We do the right thing - We are one PPD - - - -If you resonate with
our five principles above, and ultimately wish to accelerate the
delivery of safe and effective therapeutics for some of the world's
most urgent health needs, then please submit your application -
we'd love to hear from you
Keywords: Thermo Fisher Scientific, Greenville , Associate Manager/Manager CDM(Study Manager) - Remote U.S/Canada, Executive , Greenville, North Carolina
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